Ulipristal acetate
| Clinical data | |
|---|---|
| Trade names | Ella, EllaOne, Esmya, others | 
| Other names | CDB-2914; 11β-[4-(Dimethylamino)phenyl]-17α-acetoxy-19-norpregna-4,9-diene-3,20-dione | 
| AHFS/Drugs.com | Monograph | 
| License data | |
| Routes of administration  | By mouth | 
| Drug class | Selective progesterone receptor modulator | 
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | Nearly 100% | 
| Protein binding | 96.7–99.5% | 
| Metabolism | Likely CYP3A4 | 
| Elimination half-life | 32 hours | 
| Excretion | ca. 90% with feces | 
| Identifiers | |
  | |
| CAS Number | |
| PubChem CID | |
| IUPHAR/BPS | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEBI | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.207.349 | 
| Chemical and physical data | |
| Formula | C30H37NO4 | 
| Molar mass | 475.629 g·mol−1 | 
| 3D model (JSmol) | |
  | |
  | |
| (what is this?) (verify) | |
Ulipristal acetate, sold under the brand name Ella among others, is a medication used for emergency contraception (birth control) and uterine fibroids. As emergency contraception it should be used within 120 hours of vaginally penetrating intercourse. For fibroids it may be taken for up to six months. It is taken by mouth.
Common side effects include headache, nausea, feeling tired, and abdominal pain. It should not be used in women who are already pregnant. It is in the selective progesterone receptor modulator (SPRM) class of medications. It works by preventing the effects of progesterone, therefore preventing ovulation but not affecting fertilization or implantation.
Ulipristal acetate was approved for medical use in the United States in 2010. It is on the World Health Organization's List of Essential Medicines.